Design of Experiments Methodology to Build a Multifactorial Statistical Model Describing the Metabolic Interactions of Alcohol Dehydrogenase Isozymes in the Ethanol Biosynthetic Pathway of the Yeast Saccharomyces cerevisiae

被引:24
作者
Brown, Steven R. [1 ,4 ]
Staff, Marta [1 ]
Lee, Rob [2 ]
Love, John [1 ]
Parker, David A. [2 ]
Aves, Stephen J. [1 ]
Howard, Thomas P. [3 ]
机构
[1] Univ Exeter, Coll Life & Environm Sci, Biosci, Geoffrey Pope Bldg, Exeter EX4 4QD, Devon, England
[2] Shell Technol Ctr Houston, Biodomain, 3333 Highway 6 South, Houston, TX 77082 USA
[3] Newcastle Univ, Fac Sci Agr & Engn, Sch Nat & Environm Sci, Devonshire Bldg, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
[4] Synthace Ltd, London Biosci Innovat Ctr, 2 Royal Coll St, London NW1 0NH, England
来源
ACS SYNTHETIC BIOLOGY | 2018年 / 7卷 / 07期
关键词
Saccharomyces cerevisiae; ethanol biosynthesis; Design of Experiments (DOE); metabolic engineering; alcohol dehydrogenase; MACHINE LEARNING OPTIMIZATION; CHEMOSTAT CULTURES; GENES; EXPRESSION; MUTANTS;
D O I
10.1021/acssynbio.8b00112
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Multifactorial approaches can quickly and efficiently model complex, interacting natural or engineered biological systems in a way that traditional one factor-at-a-time experimentation can fail to do. We applied a Design of Experiments (DOE) approach to model ethanol biosynthesis in yeast, which is well-understood and genetically tractable, yet complex. Six alcohol dehydrogenase (ADH) isozymes catalyze ethanol synthesis, differing in their transcriptional and post-translational regulation, subcellular localization, and enzyme kinetics. We generated a combinatorial library of all ADH gene deletions and measured the impact of gene deletion(s) and environmental context on ethanol production of a subset of this library. The data were used to build a statistical model that described known behaviors of ADH isozymes and identified novel interactions. Importantly, the model described features of ADH metabolic behavior without explicit a priori knowledge. The method is therefore highly suited to understanding and optimizing metabolic pathways in less well-understood systems.
引用
收藏
页码:1676 / 1684
页数:17
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